نتایج جستجو برای: e coli expression system

تعداد نتایج: 3940018  

Journal: Vaccine Research 2014
Maryam Golshani, Payam Zandi, Saeid Bouzari,

  Introduction: Omp31 is animmunodominant and protective antigen conserved in Brucella species and a good candidate for vaccine design. Material & methods: The present study aimed at in silico design of the truncated Omp31 (TOmp31) using bioinformatic tools and to express the selected form in Escherichia coli (E. coli) Results and conclusion: Various bioinformatically calculated scores for the ...

Nasser Ghaemi Seyed Abbas Shojaosadati, Seyedeh Marjan Varedi Koolaee Valliollah Babaeipour

The objective of this research was to investigate the influence of the over-expression of recombinant interferon-g during high cell density cultivation on cellular characteristics of recombinant E. coli. Batch and fed-batch culture techniques were employed to grow Escherichia coli BL21 for production of human gamma-interferon in pET expression system. Final cell densities in batch and fed-batch...

Journal: :iranian journal of veterinary research 2011
a. derakhshandeh t. zahraei salehi m. muniesa

avian pathogenic e. coli (apec) is responsible for economic losses in all poultry farms. certain virulence factors have been proposed as a means of controlling apec infections, including some proteins to be used for vaccination. in the study we report here, one of the major virulence factors, the iss (increased serum survival) gene, from e. coli strain χ1378, isolated from poultry colibacillosi...

Journal: :medical journal of islamic republic of iran 0
mana oloomi from the molecular biology unit, pasteur institute of iran, tehran i.r. iran. saeid bouzari vladimir o rechinsky

the human granulocyte-macrophage colony stimulation factor (hgm-csf) gene was cloned in the pet 23a( +) expression vector under the control of strong bacteriophage t7 transcription and translation signals. the hgm-csf gene was transferred into e. coli strainbl21 (de3)plyss andiptg was used for induction of gm-csf gene. production of the target protein was obtained as revealed by elisa and weste...

Journal: :iranian journal of biotechnology 2015
nemat sokhandan-bashir mahin poorsmaile mohammad hajizadeh

background: the advent of recombinant dna technology has facilitated heterologous expression of proteins from various sources in different host systems including escherichia coli. if a plant virus coat protein is expressed in the bacterium it can be used as the antigen for antibody preparation. such a recombinant antigen preparation can be particularly useful where equipment such as ultracentri...

Journal: :research in pharmaceutical sciences 0
mahsa ghavim 1damghan branch, islamic azad university, damghan, i.r. iran. khalil abnous 2pharmaceutical research center, school of pharmacy, mashhad university of medical sciences, mashhad, i.r. iran. fatemeh arasteh 2pharmaceutical research center, school of pharmacy, mashhad university of medical sciences, mashhad, i.r. iran. 3department of pharmaceutical biotechnology, school of pharmacy, mashhad university of medical sciences, mashhad, i.r. iran. sahar taghavi 2pharmaceutical research center, school of pharmacy, mashhad university of medical sciences, mashhad, i.r. iran. maryam sadat nabavinia 3department of pharmaceutical biotechnology, school of pharmacy, mashhad university of medical sciences, mashhad, i.r. iran. mona alibolandi 2pharmaceutical research center, school of pharmacy, mashhad university of medical sciences, mashhad, i.r. iran.

for high-throughput production of recombinant protein in escherichia coli ( e. coli ), besides important parameters such as efficient vector with strong promoter and compatible host, other important issues including codon usage, rare codons, and gc content specially at n-terminal region should be considered. in the current study, the effect of decreasing the percentage of gc nucleotides and opt...

In this study, our previously reported novel synthetic gene encoding 166 residues of interferon-? was used for an efficient expression of IFN-?. The synthetic gene was cloned into pET21a expression vector and transferred into E. coli. Recombinant protein was over-expressed in the E. coli. Identity of the recombinant protein was confirmed by western blot analysis. The recombinant protein was bio...

Journal: :iranian biomedical journal 0
بیتا بخشی bita bakhshi مینا بوستان شناس mina boustanshenas مسعود قربانی masoud ghorbani

background: cholera toxin b subunit (ctb) has been extensively considered as an immunogenic and adjuvant protein, but its yield of expression is not satisfactory in many studies. the aim of this study was to compare the expression of native and mutant recombinant ctb (rctb) in pqe vector. methods: ctxb fragment from vibrio cholerae o1 atcc14035 containing the substitution of mutant ctxb for ami...

Journal: :jundishapur journal of microbiology 0
zahra shoja biology department, jahrom branch, islamic azad university, jahrom, ir iran hamid rajabi memari agronomy and plant breeding department, faculty of agriculture, shahid chamran university of ahvaz, ahvaz, ir iran; agronomy and plant breeding department, faculty of agriculture, shahid chamran university of ahvaz, ahvaz, ir iran. tel: +98-6133330012, fax: +98-6133330079 mohammd roayaei ardakani biology department, shahid chamran university of ahvaz, ahvaz, ir iran

conclusions over-expression of the synthetic cpc/β protein in the bacterial system (escherichia coli bl-21) showed that e. coli can be used as a basis for further research to produce this desired protein in large quantities. results the sds-page analysis and dot blotting confirmed the production of recombinant c-pc/β in the bacterial expression system. over-expression of cpcb gene was optimized...

Bita Bakhshi, Masoud Ghorbani, Mina Boustanshenas,

Background: Cholera toxin B subunit (CTB) has been extensively considered as an immunogenic and adjuvant protein, but its yield of expression is not satisfactory in many studies. The aim of this study was to compare the expression of native and mutant recombinant CTB (rCTB) in pQE vector. Methods: ctxB fragment from Vibrio cholerae O1 ATCC14035 containing the substitution of mutant ctxB for ami...

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